Clinical Research Associate

**We see human behind every number**

**Clinical Research Associate**

**Location**:**Paris/Ile-de-France area (**1-3 days/week at the client office** (day on site = office day))**

On behalf of our partner, one of the global leaders in clinical research, we are currently recruiting for a Clinical Research Associate in France (**Paris/Ile-de-France area**) to join our sponsor dedicated CRA team

You will demonstrate, **minimum 24 months independent external monitoring of commercial studies in**Cardiovascular, Renal, Metabolism and Respiratory**. Other therapeutic areas are also of interest, especially if gained on phase II-III commercial trials.

The format will be **1-3 days/week at the client office** (day on site = office day)

**As an experienced Clinical Research Associate** you will be dedicated to one of the global pharmaceutical clients.

**Detailed Job Duties and Responsibilities**
- Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.
- Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.
- Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
- Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues.
- Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.

We believe our Clinical Operations team is second to none. You will receive the support you need to develop personally and professionally and work in an environment where you matter. Our team pushes forward together. United in solving problems, developing close site relationships and reaching the end goal. Operating as a key part of a global study team, the CRA plays a fundamental role in our clients’ drug development processes.

**Education / Qualifications / Skills Requirements**
- A stable experience as a CRA, this within the pharmaceutical industry or a CRO
- **Exp in**Cardiovascular, Renal, Metabolism and Respiratory**therapeutic areas**:

- Excellent organization skills
- **Exp in RBM/RBQM** (Risk-Based Monitoring and Risk-Based Quality Management)
- Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
- Strong IT skills
- Strong communication with the ability to multitask and work effectively under pressure
- Fluency in French and professional proficiency in English

**Benefits**:

- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
- Global Employee Assistance Program
- Life assurance
- Country-specific flexible benefits, including options like gym membership discounts, childcare vouchers, and more.

KCR is a clinical development solutions provider creating value for emerging biotechnology organizations.

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